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Effectiveness of the Shock Team on Short-Term Outcomes in Patients With Cardiogenic Shock - Systematic Review and Meta-Analysis. 休克组对心源性休克患者短期预后的有效性——系统评价和荟萃分析。
IF 1.1 Pub Date : 2025-11-13 eCollection Date: 2026-01-09 DOI: 10.1253/circrep.CR-25-0240
Marina Arai, Toru Kondo, Takahiro Nakashima, Hiroyuki Hanada, Katsutaka Hashiba, Takeshi Yamamoto, Naoki Nakayama, Jin Kirigaya, Tomoko Ishizu, Yumiko Hosoya, Aya Katasako-Yabumoto, Yusuke Okazaki, Masahiro Yamamoto, Kazuo Sakamoto, Takumi Osawa, Akihito Tanaka, Kunihiro Matsuo, Junichi Yamaguchi, Toshiaki Mano, Sunao Kojima, Teruo Noguchi, Yasushi Tsujimoto, Migaku Kikuchi, Toshikazu Funazaki, Yoshio Tahara, Hiroshi Nonogi, Tetsuya Matoba

Background: Recently, shock teams have been introduced to optimize cardiogenic shock (CS) care; however, their clinical benefits remain unclear. We conducted a systematic review and meta-analysis to assess whether management by a shock team improves outcomes in patients with CS.

Methods and results: This meta-analysis was conducted according to the PRISMA guidelines. Studies comparing adults with CS managed with or without a shock team were identified from the PubMed, Web of Science, and Cochrane Library databases. The primary outcome was short-term mortality (cardiac intensive care unit, in-hospital, or 30-day mortality); the secondary outcome was bleeding. Of the 7 retrospective cohort studies that met the inclusion criteria, 3 without a critical risk of bias were included in the analysis. Shock team management was significantly associated with lower short-term mortality (odds ratio [OR] 0.52; 95% confidence interval [CI] 0.32-0.85; P=0.010) and bleeding complications (OR 0.62; 95% CI 0.43-0.91; P=0.010). Sensitivity analysis using crude data also supported the mortality benefit (OR 0.68; 95% CI 0.54-0.85; P<0.010). However, no randomized trials were included, and the certainty of evidence was rated very low owing to the risk of bias and inconsistency.

Conclusions: Shock team management may improve short-term outcomes in patients with CS; however, the level of evidence is very low. Further prospective studies are needed to evaluate optimal shock team composition and roles.

背景:最近,休克小组被引入来优化心源性休克(CS)的护理;然而,它们的临床益处尚不清楚。我们进行了一项系统回顾和荟萃分析,以评估休克小组的治疗是否能改善CS患者的预后。方法和结果:本荟萃分析按照PRISMA指南进行。从PubMed、Web of Science和Cochrane Library数据库中确定了比较有或没有休克治疗的成人CS的研究。主要终点是短期死亡率(心脏重症监护病房、住院或30天死亡率);次要结果是出血。在符合纳入标准的7项回顾性队列研究中,3项没有严重偏倚风险的研究被纳入分析。休克组管理与较低的短期死亡率(优势比[OR] 0.52; 95%可信区间[CI] 0.32-0.85; P=0.010)和出血并发症(优势比[OR] 0.62; 95%可信区间[CI] 0.43-0.91; P=0.010)显著相关。使用粗数据的敏感性分析也支持死亡率获益(OR 0.68; 95% CI 0.54-0.85)。结论:休克小组管理可能改善CS患者的短期预后,然而,证据水平非常低。需要进一步的前瞻性研究来评估最佳的冲击小组组成和作用。
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引用次数: 0
Design and Framework of JROAD-DPC - A Japanese Nationwide Registry Linking Diagnosis Procedure Combination Data With Cardiovascular Quality Metrics. JROAD-DPC的设计和框架——日本全国性的诊断程序结合数据与心血管质量指标的注册表。
IF 1.1 Pub Date : 2025-11-12 eCollection Date: 2026-01-09 DOI: 10.1253/circrep.CR-25-0217
Tatsuhiro Shibata, Koshiro Kanaoka, Yoshitaka Iwanaga, Yoko Sumita, Satoaki Matoba, Masaki Ieda, Satoshi Yasuda, Shun Kohsaka, Tetsuya Matoba, Masaharu Nakayama, Tetsuya Amano, Yasuko K Bando, Mika Enomoto, Aya Saito, Hiroshi Tada, Yoshihiro Fukumoto

Background: Comprehensive monitoring of cardiovascular disease (CVD) is essential in rapidly aging societies such as Japan. The Japanese Circulation Society (JCS) launched the Japanese Registry Of All cardiac and vascular Diseases-Diagnosis Procedure Combination (JROAD-DPC) registry, linking annual JROAD questionnaires with nationwide DPC administrative claims to enable patient-level analyses of hospitalized CVD care. This Protocol Paper presents a comprehensive overview of the registry.

Methods and results: Using anonymized data (April 2012-March 2023), we described temporal trends in patient demographics, principal CVD diagnoses, major interventions, disease-specific severity, and hospital characteristics. From FY2012-FY2022, participating facilities increased from 610 to 860, with registered patients more than doubling. Median age rose from 73.0 to 75.0 years; patients aged ≥90 years nearly quadrupled. The proportion of angina pectoris admissions declined (26.8% to 11.7%), while absolute numbers remained stable. Atrial fibrillation/flutter admissions rose in both proportion (4.1% to 5.9%) and absolute number. Heart failure admissions increased steadily, with its proportion showing a U-shaped trend. Catheter ablations for atrial fibrillation/flutter increased over fivefold, exceeding 64,000, while percutaneous coronary interventions for acute myocardial infarction surpassed 46,000.

Conclusions: JROAD-DPC now captures over 1.5 million annual CVD hospitalizations, providing a nationwide, large-scale longitudinal view of cardiovascular care in Japan. Its scale and validated coding enable robust analyses of trends and outcomes, supporting national CVD policy evaluation and improvement.

背景:全面监测心血管疾病(CVD)在日本等快速老龄化社会至关重要。日本循环学会(JCS)启动了日本所有心脏和血管疾病诊断程序组合登记(JROAD-DPC)登记,将年度JROAD问卷与全国范围内的DPC行政索赔联系起来,以便对住院心血管疾病护理进行患者层面的分析。本协议文件介绍了注册表的全面概述。方法和结果:使用匿名数据(2012年4月- 2023年3月),我们描述了患者人口统计学、主要心血管疾病诊断、主要干预措施、疾病特异性严重程度和医院特征的时间趋势。从2012财年到2022财年,参与机构从610家增加到860家,注册患者增加了一倍多。中位年龄由73.0岁上升至75.0岁;年龄≥90岁的患者几乎翻了两番。心绞痛入院比例下降(26.8%至11.7%),而绝对数字保持稳定。心房颤动/扑动住院患者的比例(4.1%至5.9%)和绝对人数均有所上升。心力衰竭入院人数稳步上升,比例呈u型趋势。房颤/扑动的导管消融增加了五倍以上,超过64,000例,而急性心肌梗死的经皮冠状动脉介入治疗超过46,000例。结论:JROAD-DPC目前每年捕获超过150万例心血管疾病住院病例,提供了日本全国范围内大规模的心血管护理纵向视图。它的规模和经过验证的编码能够对趋势和结果进行强有力的分析,支持国家心血管疾病政策的评估和改进。
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引用次数: 0
Elevated B-Type Natriuretic Peptide as a Predictor of Unfavorable Outcomes in Post-Acute Stroke Patients. b型利钠肽升高作为急性卒中后患者不良结局的预测因子
IF 1.1 Pub Date : 2025-11-11 eCollection Date: 2026-01-09 DOI: 10.1253/circrep.CR-25-0132
Genki Kai, Ken Ogura, Kensuke Ueno, Kaoru Sato, Takashi Miki, Takumi Noda, Masashi Yamashita, Masashi Kanai, Masafumi Nozoe, Kentaro Kamiya

Background: B-type natriuretic peptide (BNP) is a key biomarker for heart failure (HF) and widely used for risk stratification. Elevated BNP levels in acute stroke are linked to poor outcomes, but its prognostic value in the post-acute phase remains unclear.

Methods and results: This retrospective study included 876 patients admitted to a rehabilitation hospital after acute cerebral infarction or hemorrhage between February 2019 and December 2022. Patients were classified into 4 groups based on BNP or N-terminal prohormone of BNP. The primary outcome was all-cause unfavorable events, including in-hospital death or transfer due to worsening condition. The severely elevated BNP group had a significantly higher risk of all-cause unfavorable events (hazard ratio: 2.34; 95% confidence interval: 1.26-4.32) than the normal group. No significant difference was observed in the mildly or moderately elevated BNP groups. BNP showed superior predictive value over HF diagnosis in terms of area under the receiver operating characteristic curve (0.712 vs. 0.691), net reclassification improvement (0.304, P=0.002), and integrated discrimination improvement (0.025, P=0.015). Higher BNP was associated with lower body mass index, reduced estimated glomerular filtration rate, longer time from stroke onset, atrial fibrillation, and cardioembolic stroke.

Conclusions: BNP levels in the post-acute stroke phase were significantly associated with unfavorable outcomes and may serve as a useful prognostic marker.

背景:b型利钠肽(BNP)是心衰(HF)的关键生物标志物,被广泛用于危险分层。急性卒中中BNP水平升高与预后不良有关,但其在急性期后的预后价值尚不清楚。方法和结果:本回顾性研究纳入2019年2月至2022年12月期间入院的876例急性脑梗死或出血患者。根据BNP或n端原激素水平将患者分为4组。主要结局为全因不良事件,包括院内死亡或因病情恶化而转院。BNP严重升高组发生全因不良事件的风险显著高于正常组(风险比:2.34;95%可信区间:1.26-4.32)。轻度或中度BNP升高组无显著差异。BNP在受试者工作特征曲线下面积(0.712 vs. 0.691)、净重分类改善(0.304,P=0.002)和综合判别改善(0.025,P=0.015)方面优于HF诊断的预测价值。高BNP与较低的身体质量指数、较低的肾小球滤过率、较长的中风发病时间、心房颤动和心脏栓塞性中风相关。结论:急性卒中后阶段BNP水平与不良预后显著相关,可作为有用的预后指标。
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引用次数: 0
Effects of Rehabilitation Using Therapeutic Sandals for Patients With Chronic Limb-Threatening Ischemia. 治疗性凉鞋对慢性肢体缺血患者的康复效果。
IF 1.1 Pub Date : 2025-11-11 eCollection Date: 2026-01-09 DOI: 10.1253/circrep.CR-25-0048
Yusuke Nakamura, Takuya Hara, Manami Kurozawa, Kou Ino, Takashi Matsumoto

Background: Studies of off-loading devices for chronic limb-threatening ischemia (CLTI) are scarce. We investigated (1) the effect of the application of early therapy sandals on changes in the Clinical Frailty Scale (CFS) scores of patients with CLTI before and after hospitalization, and (2) adverse events such as wound deterioration and reamputation.

Methods and results: We retrospectively analyzed the cases of 51 patients (51 limbs) with toe amputation after revascularization and compared 2 groups: patients who did not apply any load during the off-loading duration and focused on resistance training (the 'usual rehabilitation' group), and those who used therapeutic sandals and performed walking and aerobic exercises with partial off-loading from an early stage (the 'orthotic' rehabilitation group). The before-to-after hospitalization change in the CFS score was 0 (-1, 0) in the usual rehabilitation group, and 0 (0, 1) in the orthotic rehabilitation group (P=0.002), a significant difference. There were no significant between-group differences in wound healing duration (usual rehabilitation group, 48 [19,76.5] days; orthotic rehabilitation group, 41 [27.5,78.8] days) or reamputation rate (usual rehabilitation group, 5 [22%]; orthotic rehabilitation group, 3 [11%]).

Conclusions: The early postoperative use of therapeutic sandals tended to shorten the duration of complete off-loading after toe amputation due to CLTI and to help maintain CFS scores throughout the hospitalization duration. It was also shown to have a minimal impact on treatment delay and reamputation.

背景:关于慢性肢体威胁缺血(CLTI)的卸荷装置的研究很少。我们研究了(1)早期治疗凉鞋的应用对CLTI患者住院前后临床虚弱量表(CFS)评分变化的影响,(2)伤口恶化和再截肢等不良事件的影响。方法和结果:我们回顾性分析了51例(51条肢体)经血运重建后的脚趾截肢患者,并比较了两组患者:在卸荷期间不施加任何负荷并专注于阻力训练的患者(“常规康复”组)和使用治疗性凉鞋并进行部分卸荷的步行和有氧运动的患者(“矫形”康复组)。常规康复组住院前后CFS评分变化为0(- 1,0),矫形康复组住院前后CFS评分变化为0(0,1),差异有统计学意义(P=0.002)。两组间伤口愈合时间(常规康复组,48 [19,76.5]d;矫形器康复组,41 [27.5,78.8]d)及再截肢率(常规康复组,5[22%];矫形器康复组,3[11%])差异无统计学意义。结论:术后早期使用治疗性凉鞋可缩短因CLTI引起的脚趾截肢后完全卸载的时间,并有助于在整个住院期间维持CFS评分。它也被证明对治疗延迟和再截肢的影响很小。
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引用次数: 0
Registry for Long-Term Outcomes After Catheter Ablation in Nagano Prefecture - The Shinshu Catheter Ablation (Shinshu-AB) Registry Rationale and Design. 长野县导管消融后长期结果的登记——信州导管消融(Shinshu- ab)登记的基本原理和设计。
IF 1.1 Pub Date : 2025-11-11 eCollection Date: 2026-01-09 DOI: 10.1253/circrep.CR-25-0229
Toshinori Komatsu, Ayako Okada, Hideki Kobayashi, Kiu Tanaka, Hiroaki Tabata, Wataru Shoin, Toshio Kasai, Takahiro Okano, Tatsuya Usui, Yasumasa Nohno, Ryosuke Kozu, Hideaki Sato, Takeshi Tomita, Takahiro Takeuchi, Masao Hirabayashi, Kazunori Aizawa, Yasutaka Oguchi, Yuichi Katagiri, Yasushi Wakabayashi, Koichiro Kuwahara

Background: Catheter ablation (CA) is a well-established therapy for arrhythmia, but the impact of CA strategies has not been thoroughly investigated. Nagano Prefecture comprises a large geographical area and some hospitals do not have cardiac surgeons, thus limiting the application of CA strategies. The aim of this study was to investigate the detailed strategies for CA in Nagano Prefecture and to clarify their efficacy and safety.

Methods and results: The Shinshu Catheter Ablation (Shinshu-AB) Registry is a multicenter prospective observational registry. Patients treated with CA for any type of arrhythmia are included. Data on the target arrhythmia(s), CA strategy, outcomes, and complications were collected and analyzed at Shinshu University Hospital. The study was approved by the institutional review boards of all investigational sites and registered in the UMIN Clinical Trials Registry (UMIN-55562). Primary endpoints were the composite incidence of arrhythmia recurrence, procedure-related adverse events, and cardiovascular events. The secondary endpoints were acute success, chronic success for >12 months, and all-cause death.

Conclusions: The Shinshu-AB Registry provides real-world data from the Nagano Prefecture on the outcomes and complications of CA for various types of arrhythmias.

背景:导管消融(CA)是一种公认的心律失常治疗方法,但CA策略的影响尚未得到彻底的研究。长野县的地理面积很大,一些医院没有心脏外科医生,因此限制了心脏护理战略的应用。本研究的目的是探讨长野县CA的详细策略,并阐明其有效性和安全性。方法和结果:Shinshu导管消融(Shinshu- ab)注册是一个多中心前瞻性观察注册。用CA治疗任何类型心律失常的患者都包括在内。在信州大学医院收集和分析目标心律失常、CA策略、结局和并发症的数据。该研究得到了所有研究地点的机构审查委员会的批准,并在UMIN临床试验登记处注册(UMIN-55562)。主要终点是心律失常复发、手术相关不良事件和心血管事件的综合发生率。次要终点为急性成功、慢性成功(12个月)和全因死亡。结论:Shinshu-AB Registry提供了来自长野县的关于CA治疗各种类型心律失常的结果和并发症的真实数据。
{"title":"Registry for Long-Term Outcomes After Catheter Ablation in Nagano Prefecture - The Shinshu Catheter Ablation (Shinshu-AB) Registry Rationale and Design.","authors":"Toshinori Komatsu, Ayako Okada, Hideki Kobayashi, Kiu Tanaka, Hiroaki Tabata, Wataru Shoin, Toshio Kasai, Takahiro Okano, Tatsuya Usui, Yasumasa Nohno, Ryosuke Kozu, Hideaki Sato, Takeshi Tomita, Takahiro Takeuchi, Masao Hirabayashi, Kazunori Aizawa, Yasutaka Oguchi, Yuichi Katagiri, Yasushi Wakabayashi, Koichiro Kuwahara","doi":"10.1253/circrep.CR-25-0229","DOIUrl":"10.1253/circrep.CR-25-0229","url":null,"abstract":"<p><strong>Background: </strong>Catheter ablation (CA) is a well-established therapy for arrhythmia, but the impact of CA strategies has not been thoroughly investigated. Nagano Prefecture comprises a large geographical area and some hospitals do not have cardiac surgeons, thus limiting the application of CA strategies. The aim of this study was to investigate the detailed strategies for CA in Nagano Prefecture and to clarify their efficacy and safety.</p><p><strong>Methods and results: </strong>The Shinshu Catheter Ablation (Shinshu-AB) Registry is a multicenter prospective observational registry. Patients treated with CA for any type of arrhythmia are included. Data on the target arrhythmia(s), CA strategy, outcomes, and complications were collected and analyzed at Shinshu University Hospital. The study was approved by the institutional review boards of all investigational sites and registered in the UMIN Clinical Trials Registry (UMIN-55562). Primary endpoints were the composite incidence of arrhythmia recurrence, procedure-related adverse events, and cardiovascular events. The secondary endpoints were acute success, chronic success for >12 months, and all-cause death.</p><p><strong>Conclusions: </strong>The Shinshu-AB Registry provides real-world data from the Nagano Prefecture on the outcomes and complications of CA for various types of arrhythmias.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 1","pages":"174-179"},"PeriodicalIF":1.1,"publicationDate":"2025-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12783018/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145954834","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Association Between Fatty Liver Index and Brachial-Ankle Pulse Wave Velocity in the General Population - A Cross-Sectional Study. 在一般人群中,脂肪肝指数与臂踝脉搏波速度的关系——一项横断面研究。
IF 1.1 Pub Date : 2025-11-08 eCollection Date: 2026-01-09 DOI: 10.1253/circrep.CR-25-0218
Daisuke Tokutake, Yuichi Akasaki, Shuya Shinchi, Shota Uebo, Shin Kawasoe, Takuro Kubozono, Hironori Miyahara, Koichi Tokushige, Mitsuru Ohishi

Background: Although metabolic dysfunction-associated fatty liver disease is typically diagnosed using ultrasonography, the fatty liver index (FLI) offers a simple alternative. Brachial-ankle pulse wave velocity (baPWV) is an established marker of arterial stiffness and a predictor of cardiovascular events. This study investigated the association between FLI and baPWV in a general Japanese population.

Methods and results: This cross-sectional study included participants aged ≥18 years, excluding those with atrial fibrillation, lower extremity artery disease, severe aortic stenosis, or missing data. The primary outcome was an elevated baPWV (≥1,800 cm/s). Multivariable logistic regression analysis was performed to assess the association between FLI and elevated baPWV, considering FLI both as a categorical variable (low risk: FLI <30; moderate risk: FLI ≥30 and <60; high risk: FLI ≥60) and as a continuous variable (per 10-unit increase). The analysis included 10,122 individuals (mean age 54.3 years; 55% male). In multivariable-adjusted models, the odds of elevated baPWV were significantly higher in the moderate-risk (odds ratio [OR] 1.47; 95% confidence interval [CI] 1.20-1.79) and high-risk (OR 1.78; 95% CI 1.33-2.38) groups, using the low-risk group as the reference category. Each 10-unit increase in FLI was associated with significantly higher odds of the outcome (OR 1.16; 95% CI 1.10-1.22).

Conclusions: FLI showed a significant association with arterial stiffness in the general Japanese population.

背景:虽然代谢功能障碍相关的脂肪肝疾病通常使用超声诊断,但脂肪肝指数(FLI)提供了一种简单的替代方法。肱-踝关节脉搏波速度(baPWV)是动脉僵硬度和心血管事件的预测指标。本研究调查了日本普通人群中FLI和baPWV之间的关系。方法和结果:这项横断面研究纳入了年龄≥18岁的参与者,排除了房颤、下肢动脉疾病、严重主动脉狭窄或数据缺失的患者。主要终点为baPWV升高(≥1800 cm/s)。多变量logistic回归分析评估FLI和baPWV升高之间的关系,考虑FLI作为一个分类变量(低风险:FLI)。结论:FLI在一般日本人群中显示出动脉僵硬的显著相关性。
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引用次数: 0
Impacts of Sarcopenia, Osteopenia, and Osteosarcopenia on Patients Undergoing Transcatheter Aortic Valve Implantation - A Single-Center Retrospective Cohort Study. 经导管主动脉瓣植入术患者肌少症、骨质减少症和骨少症的影响——一项单中心回顾性队列研究
IF 1.1 Pub Date : 2025-11-08 eCollection Date: 2026-01-09 DOI: 10.1253/circrep.CR-25-0190
Hiroshi Kurazumi, Ryo Suzuki, Takato Nakashima, Ryosuke Nawata, Toshiki Yokoyama, Kazumasa Matsunaga, Yosuke Miyazaki, Atsuo Yamashita, Takayuki Okamura, Akihito Mikamo, Motoaki Sano, Kimikazu Hamano

Background: The advent of transcatheter aortic valve implantation (TAVI) has increased the rate of aortic valve treatment in frail older adults. Factors contributing to frailty include sarcopenia (characterized by reduced muscle mass), osteopenia (characterized by decreased bone mineral density), and the newly termed osteosarcopenia, which is characterized by a simultaneous decline in muscle mass and bone mineral density. In this study, we aimed to investigate the impacts of sarcopenia, osteopenia, and osteosarcopenia on the clinical outcomes of TAVI.

Methods and results: We retrospectively analyzed 490 patients who underwent TAVI for aortic stenosis at Yamaguchi University Hospital between April 2014 and March 2025. Osteopenia, sarcopenia, and osteosarcopenia were diagnosed by preprocedural computed tomography. Patients were classified into normal (N), sarcopenia alone (S), osteopenia alone (O), and osteosarcopenia (OS) groups. Early clinical outcomes and 1-year survival rates exhibited no significant differences among the groups. However, the 5-year survival rates were 94.1%, 77.6%, 60.4%, and 46.5% in the N, S, O, and OS groups, respectively (P<0.05). The Cox proportional hazards model revealed osteosarcopenia as a significant risk factor for late death (hazard ratio, 2.09; P=0.0002).

Conclusions: Preoperative evaluation of muscle mass and bone density aids in stratifying TAVI risk.

背景:经导管主动脉瓣植入术(TAVI)的出现增加了体弱老年人主动脉瓣治疗的比率。导致虚弱的因素包括肌肉减少症(以肌肉量减少为特征)、骨质减少症(以骨密度下降为特征)和新命名的骨骨量减少症,其特征是肌肉量和骨密度同时下降。在本研究中,我们旨在探讨肌肉减少症、骨质减少症和骨骼肌减少症对TAVI临床结果的影响。方法和结果:我们回顾性分析了2014年4月至2025年3月期间在山口大学医院接受主动脉瓣狭窄TAVI治疗的490例患者。手术前计算机断层扫描诊断为骨质减少、肌肉减少和骨骼肌减少。将患者分为正常组(N)、单纯肌肉减少组(S)、单纯骨质减少组(O)和骨质减少组(OS)。两组间的早期临床结果和1年生存率无显著差异。然而,N、S、O和OS组的5年生存率分别为94.1%、77.6%、60.4%和46.5%(结论:术前评估肌肉质量和骨密度有助于TAVI风险分层。
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引用次数: 0
Comparative Efficacy of Noradrenaline vs. Other Vasopressors on Outcomes in Patients With Cardiogenic Shock - A Systematic Review and Meta-Analysis. 去甲肾上腺素与其他血管加压药物对心源性休克患者预后的比较疗效——一项系统综述和荟萃分析。
IF 1.1 Pub Date : 2025-11-07 eCollection Date: 2025-12-10 DOI: 10.1253/circrep.CR-25-0188
Yumiko Hosoya, Masahiro Yamamoto, Hiroyuki Hanada, Takumi Osawa, Marina Arai, Kazuo Sakamoto, Yusuke Okazaki, Aya Katasako-Yabumoto, Tomoko Ishizu, Toru Kondo, Jin Kirigaya, Naoki Nakayama, Takeshi Yamamoto, Katsutaka Hashiba, Takahiro Nakashima, Teruo Noguchi, Yasushi Tsujimoto, Migaku Kikuchi, Toshikazu Funazaki, Yoshio Tahara, Hiroshi Nonogi, Tetsuya Matoba

Background: Because the optimal choice of vasopressor for the initial treatment of cardiogenic shock (CS) remains controversial, we conducted a systematic review and meta-analysis to evaluate whether noradrenaline improves clinical outcomes compared with other vasopressors (adrenaline, dopamine, and vasopressin) in patients with CS.

Methods and results: PubMed, CENTRAL, and Web of Science databases were searched for randomized controlled trials (RCTs) and observational studies comparing noradrenaline with other vasopressors in adults with CS. A meta-analysis was conducted using fixed-effect models where appropriate. Two RCTs were included (n=337). One trial enrolled 57 patients and compared the effects of noradrenaline and adrenaline. Another study included 280 patients with CS as a subgroup and compared noradrenaline with dopamine. Pooled analysis showed that noradrenaline likely reduced the 28-day mortality rate compared with other vasopressors (very-low certainty). This corresponded to approximately 110 fewer deaths per 1000 patients (95% confidence interval: 217 fewer to 5 fewer). Secondary outcomes from the Levy study indicated fewer adverse events in the noradrenaline group.

Conclusions: Noradrenaline likely reduces the 28-day mortality rate compared with other vasopressors (very-low certainty) in CS. Given the small number of studies and the potential bias, further large-scale trials are warranted.

背景:由于心脏源性休克(CS)初始治疗血管加压素的最佳选择仍然存在争议,我们进行了一项系统回顾和荟萃分析,以评估与其他血管加压素(肾上腺素、多巴胺和血管加压素)相比,去甲肾上腺素是否能改善CS患者的临床结果。方法和结果:检索PubMed、CENTRAL和Web of Science数据库,查找随机对照试验(rct)和观察性研究,比较去甲肾上腺素与其他血管加压药物在成人CS中的作用。适当时使用固定效应模型进行meta分析。纳入两项随机对照试验(n=337)。一项试验招募了57名患者,比较去甲肾上腺素和肾上腺素的效果。另一项研究将280名CS患者作为亚组,并将去甲肾上腺素与多巴胺进行比较。综合分析显示,与其他血管加压药物相比,去甲肾上腺素可能降低28天死亡率(非常低的确定性)。这相当于每1000名患者死亡人数减少约110人(95%置信区间:减少217人至减少5人)。利维研究的次要结果表明,去甲肾上腺素组的不良事件较少。结论:与其他血管加压药物相比,去甲肾上腺素可能降低CS患者的28天死亡率(非常低的确定性)。考虑到研究数量少和潜在的偏倚,进一步的大规模试验是有必要的。
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引用次数: 0
Implementation of an Enteral Nutrition Protocol in the Cardiac Care Unit - A Retrospective Study of Critically Ill Cardiovascular Patients. 在心内科实施肠内营养方案——对危重心血管患者的回顾性研究。
IF 1.1 Pub Date : 2025-11-05 eCollection Date: 2026-01-09 DOI: 10.1253/circrep.CR-25-0113
Tadakiyo Ido, Takaharu Hayashi, Tomoki Yamada, Kei Nakamoto, Yohei Sotomi, Yoshiharu Higuchi

Background: Enteral nutrition (EN) is often delayed in critically ill cardiovascular patients due to concerns about bowel ischemia, especially when under vasopressor or mechanical support. We evaluated the impact of a structured EN protocol designed to promote timely and safe nutrition delivery in the Cardiac Care Unit (CCU).

Methods and results: This single-center retrospective study compared mechanically ventilated CCU patients before (April 2019-March 2020) and after (April 2022-March 2023) protocol implementation. The protocol specified hemodynamic safety thresholds and used a peptide-based formula. Outcomes included EN-related complications, time to EN initiation, and nutritional adequacy within the first week. A total of 116 patients (58 per group) were analyzed. No significant differences were observed in vomiting (P=0.717), diarrhea (P=0.219), or bowel ischemia (P=0.364). The post-protocol group showed a significantly shorter time to EN initiation (median 39.5 vs. 76.0 h; P<0.001). By Day 5, enteral energy adequacy improved (40.8% vs. 12.3%; P<0.001), and protein adequacy increased (62.2% vs. 31.0%; P<0.001). Exploratory analyses showed no significant differences in CCU stay, ventilator-free days, or in-hospital deaths.

Conclusions: The EN protocol enabled earlier initiation and improved EN delivery in high-risk CCU patients without increasing complications, offering a safe and practical approach to narrowing the gap between guidelines and practice.

背景:由于担心肠缺血,肠内营养(EN)在危重心血管患者中经常被延迟,特别是在血管加压或机械支持下。我们评估了一个结构化的EN方案的影响,该方案旨在促进心脏护理病房(CCU)及时和安全的营养输送。方法和结果:本单中心回顾性研究比较了机械通气CCU患者在方案实施前(2019年4月- 2020年3月)和实施后(2022年4月- 2023年3月)的情况。该方案规定了血流动力学安全阈值,并使用了基于肽的配方。结果包括EN相关并发症、EN起始时间和第一周内的营养充足性。共分析116例患者(每组58例)。呕吐(P=0.717)、腹泻(P=0.219)、肠缺血(P=0.364)无显著性差异。方案后组的EN起始时间明显缩短(中位数为39.5 h vs. 76.0 h)。结论:EN方案能够在不增加并发症的情况下使高危CCU患者更早起始并改善EN交付,为缩小指南与实践之间的差距提供了一种安全实用的方法。
{"title":"Implementation of an Enteral Nutrition Protocol in the Cardiac Care Unit - A Retrospective Study of Critically Ill Cardiovascular Patients.","authors":"Tadakiyo Ido, Takaharu Hayashi, Tomoki Yamada, Kei Nakamoto, Yohei Sotomi, Yoshiharu Higuchi","doi":"10.1253/circrep.CR-25-0113","DOIUrl":"10.1253/circrep.CR-25-0113","url":null,"abstract":"<p><strong>Background: </strong>Enteral nutrition (EN) is often delayed in critically ill cardiovascular patients due to concerns about bowel ischemia, especially when under vasopressor or mechanical support. We evaluated the impact of a structured EN protocol designed to promote timely and safe nutrition delivery in the Cardiac Care Unit (CCU).</p><p><strong>Methods and results: </strong>This single-center retrospective study compared mechanically ventilated CCU patients before (April 2019-March 2020) and after (April 2022-March 2023) protocol implementation. The protocol specified hemodynamic safety thresholds and used a peptide-based formula. Outcomes included EN-related complications, time to EN initiation, and nutritional adequacy within the first week. A total of 116 patients (58 per group) were analyzed. No significant differences were observed in vomiting (P=0.717), diarrhea (P=0.219), or bowel ischemia (P=0.364). The post-protocol group showed a significantly shorter time to EN initiation (median 39.5 vs. 76.0 h; P<0.001). By Day 5, enteral energy adequacy improved (40.8% vs. 12.3%; P<0.001), and protein adequacy increased (62.2% vs. 31.0%; P<0.001). Exploratory analyses showed no significant differences in CCU stay, ventilator-free days, or in-hospital deaths.</p><p><strong>Conclusions: </strong>The EN protocol enabled earlier initiation and improved EN delivery in high-risk CCU patients without increasing complications, offering a safe and practical approach to narrowing the gap between guidelines and practice.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 1","pages":"127-135"},"PeriodicalIF":1.1,"publicationDate":"2025-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12782910/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145954837","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Long-Term Implantable Biventricular Assist Device Support - Experience of 6 Cases. 长期植入式双心室辅助装置支持6例体会。
IF 1.1 Pub Date : 2025-11-05 eCollection Date: 2026-01-09 DOI: 10.1253/circrep.CR-25-0224
Shusuke Imaoka, Shunsuke Saito, Daisuke Yoshioka, Takuji Kawamura, Ai Kawamura, Shin Yajima, Ryohei Matsuura, Yusuke Misumi, Shigeru Miyagawa

Background: Managing heart failure complicated by severe right heart failure with implantable mechanical circulatory support remains a significant challenge. One therapeutic strategy is biventricular assist device (BiVAD) support, typically involving the off-label use of 2 implantable left ventricular assist devices (LVADs). Because the available data of implantable BiVAD support remain limited, we reviewed the data for 6 patients on implantable BiVAD support.

Methods and results: Between January 2010 and March 2019, 6 patients underwent BiVAD implantation at Osaka University Hospital. Their mean age was 31±11 years, and 2 (33%) were male. The right ventricular assist devices (RVADs) utilized were Jarvik2000 (Jarvik Heart, NY, USA) in 4 patients (67%), and HVAD (HeartWare, Framingham, MA, USA) in 2 patients (33%). The survival rates at 1 and 3 years after BiVAD implantation were 83% and 67%, respectively. Of the 6 patients, 4 underwent heart transplantation at 553, 709, 791, and 1,245 days, respectively, following RVAD implantation; 2 patients died during follow-up at 280 and 511 days, respectively, after RVAD implantation. Stroke occurred in 3 patients. Hemolysis or pump thrombosis occurred in 3 patients. Heart failure occurred in 3 patients. Device-related infection occurred in 1 patient.

Conclusions: Although implantable BiVAD support provided a feasible bridge to transplantation with favorable survival, the high incidence of complications indicates that significant challenges remain in optimizing patient outcomes and emphasizes the necessity for RV-specific device development.

背景:用植入式机械循环支持系统治疗心力衰竭合并严重右心衰仍然是一个重大挑战。一种治疗策略是双心室辅助装置(BiVAD)支持,通常包括2个植入式左心室辅助装置(lvad)的非适应症使用。由于植入式BiVAD支持的可用数据仍然有限,我们回顾了6例植入式BiVAD支持患者的数据。方法与结果:2010年1月至2019年3月,6例患者在大阪大学医院接受BiVAD植入。平均年龄31±11岁,男性2例(33%)。使用的右心室辅助装置(rvad)有4例(67%)为Jarvik2000 (Jarvik Heart, NY, USA), 2例(33%)为HVAD (HeartWare, Framingham, MA, USA)。BiVAD植入后1年和3年生存率分别为83%和67%。在6名患者中,4名患者分别在RVAD植入后553、709、791和1245天接受了心脏移植;2例患者分别在RVAD植入后280天和511天的随访中死亡。3例发生脑卒中。3例发生溶血或泵血栓形成。3例患者发生心力衰竭。1例患者发生器械相关感染。结论:尽管植入式BiVAD支持为移植提供了一个可行的桥梁,具有良好的生存率,但高发生率的并发症表明,在优化患者预后方面仍存在重大挑战,并强调了rv专用设备开发的必要性。
{"title":"Long-Term Implantable Biventricular Assist Device Support - Experience of 6 Cases.","authors":"Shusuke Imaoka, Shunsuke Saito, Daisuke Yoshioka, Takuji Kawamura, Ai Kawamura, Shin Yajima, Ryohei Matsuura, Yusuke Misumi, Shigeru Miyagawa","doi":"10.1253/circrep.CR-25-0224","DOIUrl":"10.1253/circrep.CR-25-0224","url":null,"abstract":"<p><strong>Background: </strong>Managing heart failure complicated by severe right heart failure with implantable mechanical circulatory support remains a significant challenge. One therapeutic strategy is biventricular assist device (BiVAD) support, typically involving the off-label use of 2 implantable left ventricular assist devices (LVADs). Because the available data of implantable BiVAD support remain limited, we reviewed the data for 6 patients on implantable BiVAD support.</p><p><strong>Methods and results: </strong>Between January 2010 and March 2019, 6 patients underwent BiVAD implantation at Osaka University Hospital. Their mean age was 31±11 years, and 2 (33%) were male. The right ventricular assist devices (RVADs) utilized were Jarvik2000 (Jarvik Heart, NY, USA) in 4 patients (67%), and HVAD (HeartWare, Framingham, MA, USA) in 2 patients (33%). The survival rates at 1 and 3 years after BiVAD implantation were 83% and 67%, respectively. Of the 6 patients, 4 underwent heart transplantation at 553, 709, 791, and 1,245 days, respectively, following RVAD implantation; 2 patients died during follow-up at 280 and 511 days, respectively, after RVAD implantation. Stroke occurred in 3 patients. Hemolysis or pump thrombosis occurred in 3 patients. Heart failure occurred in 3 patients. Device-related infection occurred in 1 patient.</p><p><strong>Conclusions: </strong>Although implantable BiVAD support provided a feasible bridge to transplantation with favorable survival, the high incidence of complications indicates that significant challenges remain in optimizing patient outcomes and emphasizes the necessity for RV-specific device development.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 1","pages":"103-109"},"PeriodicalIF":1.1,"publicationDate":"2025-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12782911/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145954765","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Circulation reports
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